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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

666111.0-S1 — Class IIb MDR by VTI Ventil Technik GmbH

MD Atlas
VTI Ventil Technik GmbH

EUDAMED last updated this device on May 28, 2026

666111.0-S1

4066206400005Q

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VTI Ventil Technik GmbH
UDI-DI code: 04066206400019
Reference / catalog number: 666111.0-S1

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View device family (Basic UDI)

Manufacturer information

Organization name: VTI Ventil Technik GmbH
SRN: DE-MF-000006534
Manufacturer status: Active

Related devices

666343.0-S14066206400005QOn the market 666312.0-S24066206400005QOn the market 666342.0-S24066206400005QOn the market 666243D.0-S24066206400005QOn the market 666343.0-S24066206400005QOn the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jul 11, 2007	May 28, 2026

Device identification

Trade name: not provided
UDI-DI code: 04066206400019
Basic UDI-DI: 4066206400005Q
Reference / catalog number: 666111.0-S1
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Ventil mit integrierten Druckregler
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04066206400019

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

R9080RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.